Inhibitors of protein prenyltransferases

ABSTRACT

The present invention is directed to novel compounds. These compounds can be useful in inhibiting the activity of GGTase I. The compounds can also be used as anti-cancer therapeutics including as part of methods for treating cancer, in assays, and in kits.

Embodiments of the present invention were made with Government support of Grant No. CA32737, awarded by the NIH. The Government may have certain rights in this invention.

BACKGROUND

Certain protein prenyltransferases have been implicated in cancer processes. Two such prenyltransferases, protein farnesyltransferase (FTase) and protein geranylgeranyltransferase type I (GGTase I) are regarded as structurally similar enzymes. See Protein Lipidation (2001) The Enzymes vol. 21. (eds. Tamanoi, F. and Sigman D. S.) Academic Press. FTase consists of two subunits, alpha and beta. Its structure consists exclusively of alpha helices and the alpha subunit wraps around the beta subunit that forms a beta-beta barrel structure. GGTase I is also a heterodimer containing an alpha-subunit that is shared with FTase. Furthermore, the beta-subunit of GGTase I shares a significant similarity with the beta-subunit of FTase.

FTase catalyzes the transfer of a C15 farnesyl group from farnesyl pyrophosphate, an intermediate in cholesterol biosynthesis, to proteins such as Ras, Rheb, nuclear lamins, CENP-E, F and protein tyrosine phosphatases pRL1-3. See Tamanoi, F., Gau, C. L., Edamatsu, H., Jiang, C. and Kato-Stankiewicz, J. (2001) Protein farnesylation in mammalian cells, Cell Mol. Life. Sci. 58, 1-14. These proteins end with the CaaX motif that is recognized by FTase.

GGTase I catalyzes the transfer of a C20 geranylgeranyl group from geranylgeranyl pyrophosphate to proteins ending with the CaaL motif. Geranylgernaylated proteins include Rho, Rac, Cdc42 as well as gamma-subunit of heterotrimeric G-proteins.

The significance of FTase and GGTase I to cancer has been addressed in the past decade. See Tamanoi, F., Gau, C. L., Edamatsu, H., Jiang, C. and Kato-Stankiewicz, J. (2001) Protein farnesylation in mammalian cells, Cell Mol. Life Sci. 58, 1-14; Carrico, D., Blaskovich, M. A., Bucher, C. J., Sebti, S. M., Hamilton, A. D. (2005) Design, synthesis, and evaluation of potent and selective benzoyleneurea-based inhibitors of protein geranylgeranyltransferase-I, Bioorg. Med. Chem. 13, 677-688; Peterson, Y. K., Kelly, P., Weinbaum, C. A., Casey, P. J. (2006) A Novel Protein Geranylgeranyltransferase-I Inhibitor with High Potency, Selectivity and Cellular Activity, J. Biol. Chem.

A number of small molecule inhibitors of FTase have been developed and some of these are currently in clinical trials as anti-cancer therapeutics. See O'Regan, R. M., Khuri, F. R. (2004) Farnesyl transferase inhibitors: the next targeted therapies for breast cancer? Endocr. Relat. Cancer 11, 191-205; ClinicalTrials.gov:www.clinicaltrials.gov. Farnesyltransferase inhibitors (FTIs) exhibit clinical activities with leukemia, multiple myeloma, glioblastoma and advanced breast cancer. Ras proteins are farnesylated and that farnesylation and membrane association of the Ras proteins is critical for their ability to transform cells. Preclinical studies using mouse model systems driven by activated H-ms revealed dramatic ability of FTIs to inhibit tumor growth. However, subsequent studies demonstrated that FTIs are incapable of inhibiting prenylation of K-ras4B and N-ras, as these proteins are alternatively modified by geranylgeranyltransferase type I in the presence of FTIs. Thus, the effects of FTIs are speculated to be due to the inhibition of other farnesylated proteins such as Rheb, CENP-E, F, RhoB.

Compared with FTIs, development of geranylgeranyltransferase type I inhibitors (GGTIs) has lagged behind. Only a handful of compounds has been identified and most of these are derived from the CaaL peptide. See (a) Farnesyltransferase inhibitors in cancer therapy (eds. Sebti, S. M. and Hamilton, A. D.) Humana Press. (b) Oualid, F. E., van den Elst, H., Leroy, I. M., Pieterman, E., Cohen, L. H., Burm, B. E. A., Overkleeft, H. S., van der Marel, G. A., Overhand, M. (2005) A Combinatorial Approach toward the Generation of Ambiphilic Peptide-Based Inhibitors of Protein:Geranylgeranyl Transferase-I, J. Comb. Chem. 7, 703-713. (c) Carrico, D., Blaskovich, M. A., Bucher, C. J., Sebti, S. M., Hamilton, A. D. (2005) Design, synthesis, and evaluation of potent and selective benzoyleneurea-based inhibitors of protein geranylgeranyltransferase-I, Bioorg. Med. Chem. 13, 677-688. (d) Peterson, Y. K., Kelly, P., Weinbaum, C. A., Casey, P. J. (2006) A Novel Protein Geranylgeranyltransferase-I Inhibitor with High Potency, Selectivity and Cellular Activity, J. Biol. Chem.

Chemical genomics intends to identify small molecule inhibitors of medically relevant targets in a systematic manner. While there are more than 100,000 proteins in the human body and approximately 10% of these are involved in human disease, only 500 have been exploited as drug targets. Thus, a vast amount of novel targets are present and identification of small molecule inhibitors of these unknown targets is of paramount importance. To maximize the chance of identifying small molecule compounds against these targets, a variety of libraries that have diverse structural motifs are needed. This is the goal of diversity-oriented synthesis (DOS). In contrast to combinatorial chemistry that aims to create a library of compounds derived from one scaffold, DOS aims to generate an array of compounds with different three-dimensional structures. See (a) Richter, H.; Walk, T.; Höltzel, A.; Jung, G. “Polymer Bound 3-Hydroxy-2-methylidenepropionic Acids. A Template for Multiple Core Structure Libraries” J. Org. Chem. 1999, 64, 1362-1365. (b) Purandare, A. V.; Gao, A.; Poss, M. A. “Solid-phase synthesis of ‘diverse’ heterocycles” Tetrahedron Lett. 2002, 43, 3903-3906. (c) Huang, X.; Liu, Z. “Solid-Phase synthesis of 4(1H)-Quinolone and Pyrimidine Derivatives Based on a New Scaffold-Polymer-Bound Cyclic Malonic Acid Ester” J. Org. Chem. 2002, 67, 6731-6737. (d) Couladouros E. A.; Strongilos, A. T. “Generation of Libraries of Pharmacophoric Structures with Increased Complexity and Diversity by Employing Polymorphic Scaffolds” Angew. Chem. Int. Ed. 2002, 41, 3677-3680. (e) Bertozzi, F.; Gundersen, B. V.; Gustafsson, M.; Olsson, R. “A Combinatorial Scaffold Approach Based upon a Multicomponent Reaction” Org. Lett. 2003; 5, 1551-1554. (f) Taylor, S. J.; Taylor, A. M.; Schreiber, S. L. “Synthetic Strategy toward Skeletal Diversity via Solid-Supported, Otherwise Unstable Reactive Intermediates” Angew. Chem. Int. Ed. 2004, 43, 1681-1685.

Diversity-oriented synthesis of chemical compound library provides a powerful means to identify small molecule inhibitors against medically relevant targets. Initial screens of a pilot library followed by diversification using solid phase synthesis can yield potent inhibitors of enzymes in a relatively short period of time.

Since late 1990, a number of attempts to carry out diversity-oriented synthesis have been reported. One example is the use of squaric acid as a multireactive core molecule to generate a library consisting of different core structures. See Tempest, P. A. and Armstrong, R. W. (1997) Cyclobutenedione derivatives on solid support: Toward multiple core structure libraries. J. Am. Chem. Soc. 119, 7607-7608. However, very few of these examples were used in actual library synthesis. See (a) Ding, S.; Gray, N. S.; Wu, X.; Ding, Q.; Schultz, P. G. “A Combinatorial Scaffold Approach toward Kinase-Directed Heterocycle Libraries” J. Am. Chem. Soc. 2002, 124, 1594-1596. (b) Kwon, O.; Park, S. B.; Schreiber, S. L. “Skeletal Diversity via a Branched Pathway Efficient Synthesis of 29,400 Discrete, Polycyclic Compounds and Their Arraying into Stock Solutions” J. Am. Chem. Soc. 2002, 124, 13402-13404. (c) Burke, M. D.; Berger, E. M.; Schreiber, S. L. “Generating Diverse Skeletons of Small Molecules Combinatorially” Science 2003, 302, 613-618. Due to drastically different reaction conditions, the yields greatly varied from one reaction to another, which discouraged adaptation of the methodology to a combinatorial library synthesis in solid-phase.

There thus exists a need for the identification of a multireactive core molecule for which more consistent reaction conditions can be used and with which more consistent yield is obtained in diversity oriented synthesis. There exists a need for novel GGTI compounds. There exists a need for GGTIs that are specific against K-Ras4B.

SUMMARY

Some exemplary embodiments of the invention are directed to compounds having the formula:

wherein J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen,

wherein G is

wherein E is selected from the group consisting of hydrogen, C₁-C₃ alkyl, and halogen,

wherein W is selected from the group consisting of cyclic, linear, or branched alkyl of from 2 to 8 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen,

wherein X—Y is selected from the group consisting of

wherein A is selected from the group consisting of

and —CO₂M;

wherein M is selected from the group consisting of hydrogen and alkyl of from 1 to 2 carbons,

“wherein n is between 0 and 3 carbons;

wherein R is any alpha-substituent of an amino acid;

wherein Z is S—U; and

wherein U is selected from the group consisting of alkyl of from 2 to 10 carbons; and salts of the compound.

Some exemplary embodiments of the invention are directed to a compound or salt thereof having the formula:

Some exemplary embodiments of the invention are directed to a compound or salt thereof having the formula:

Some exemplary embodiments of the invention are directed to a compound having the formula:

In some exemplary embodiments of the invention the compound or a salt thereof inhibits the activity of a protein prenyltransferase. The invention is also directed to pharmaceutical compositions comprising the compound or salt of the invention and a pharmaceutically acceptable carrier or diluent.

Some exemplary embodiments of the invention are directed a method comprising administering the compound or salt of the invention to a cell in an amount sufficient to inhibit the activity of GGTase I.

Some exemplary embodiments of the invention are directed a method comprising administering a compound or salt of the invention in an amount sufficient to inhibit the growth of a cancer cell. The cancer can be, but is not limited, pancreatic, leukemia, breast, lung, colon, ovarian, stomach, and prostate cancer. In some embodiments, the cancer cell comprises GGTase I modified proteins.

Some exemplary embodiments of the invention are directed a method comprising administering to a subject in need of treatment for a cancer a pharmaceutical composition of the present invention in an amount sufficient to inhibit the activity of a protein prenyltransferase.

Some exemplary embodiments of the invention are directed a method comprising measuring the GGTase I inhibiting activity of a compound of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 presents a pilot library of compounds.

FIG. 2 presents the structure of GGTIs identified from the pilot library.

FIG. 3 illustrates that GGTI effects are not influenced by the addition of detergents.

FIG. 4 presents the structure of FTIs identified from the pilot library.

FIG. 5 presents an illustration of synthetic steps. The steps may include (a) allenoic acid, Mukaiyama's reagent, DIPEA or Et₃N, DCM, room temperature, for 12 hours; (b) PPH₃ or PBu₃, imine, benzene or DCM at room temperature or 60° C.; (c) 2.5% TFA/DCM for 12 hours; (d) thiol, n-BuLi, at −25° C., THF.

FIG. 6 presents illustrations of chemical steps in building block preparation.

FIG. 7 presents γ-substituted allenoic acid building blocks.

FIG. 8 presents α-substituted allenoic acid building blocks.

FIG. 9 presents N-sulfonylimine building blocks.

FIG. 10 presents thiol building blocks.

FIGS. 11A-H present structures and numbers of the library compounds.

FIG. 12 presents tetrahydropyridine scaffold compounds with GGTI activity.

FIG. 13 presents piperidine scaffold compounds with GGTI activity.

FIG. 14 presents piperidine scaffold compounds with GGTI activity.

FIGS. 15A and 15B present dose dependency of GGTase I inhibition by two GGTI compounds.

FIG. 16 presents a comparison of GGTase inhibition and FTase inhibition by three compounds.

FIGS. 17A and 17B present GGTI compounds with preferential inhibition of K-Ras4B-driven GGTase I activity.

FIG. 18 presents focused future libraries based on SAR analysis.

FIGS. 19-1 through 19-27 present the measured Kras inhibitory activities of individual compounds.

FIGS. 20A-20C illustrate specific inhibition of GGTase I by P3-E5 and P5-H6. FIGS. 20D-F show the structure of GGTase I (D), FTase (E) and GGTase II (F).

FIGS. 21A-21D illustrate that GGTIs compete with substrate protein but do not compete with GGPP, with a scheme shown in 21E.

FIGS. 22A and 22B show inhibition of gernaylgeranylation in cells treated with P3-E5.

FIG. 23 illustrates inhibition of proliferation in K562 cells by GGTIs.

FIG. 24A illustrates that GGTIs induce G1 cell cycle arrest in K562 cells with a scheme shown in 24B.

FIGS. 25A and 25B illustrate that mP5-H6 inhibits geranylgeranylation in vivo.

FIG. 26 illustrates that mP5-H6 exhibits increased potency to inhibit proliferation of Panc-1 and Jurkat cells.

FIG. 27 illustrates exemplary GGTIs of the present invention (mP5-H6, P5-H6, and P3-E5) and some other GGTI compounds.

FIG. 28 illustrates structures of GGTIs with dihydropyrrole scaffold 6.

FIGS. 29A to 29C illustrate structures of GGTIs with pyrrolidine scaffold 10.

FIGS. 30A to 30E illustrate structures and members of a library of compounds.

FIG. 31 illustrates a method of synthesizing GGTIs.

FIG. 32 illustrates a formula for exemplary compounds of the present invention.

FIG. 33 shows Western blots of cell lysates with geranylgeranylated Rheb, using compounds 22 and 23.

DETAILED DESCRIPTION

Embodiments of the invention are discussed in detail below. In describing embodiments, specific terminology is employed for the sake of clarity. However, the invention is not intended to be limited to the specific terminology so selected. A person skilled in the relevant art will recognize that other equivalent parts can be employed and other methods developed without parting from the spirit and scope of the invention. All references cited herein are incorporated by reference as if each had been individually incorporated.

There are several reasons that GGTase I is also an attractive target of anti-cancer drug development. First, Rho proteins such as RhoA and Rac are critical in enhancing transformation. In fact, peptidomimetic inhibitors of GGTase I have shown promise in inhibiting proliferation of cancer cells. An arrest of the cell cycle at the G0/G1 phase was consistently observed with GGTase I inhibitors.

Second, one of the geranylgeranylated proteins, RhoC, has been identified as a protein involved in cancer metastasis. See (a) Clark, E. A., Golub, T. R., Lander, E. S. and Hynes, R. O. (2000) Genomic analysis of metastasis reveals an essential role for RhoC. Nature 406, 466-467. (b) Hakem, A., Sanchez-Sweatman, You-Ten, A., Duncan, G., Wakeham, A., Khokha, R. and Mak, T. W. (2005) RhoC is dispensable for embryogenesis and tumor initiation but essential for metastasis. Genes & Develop. 19, 1974-1979. Thus, blocking the function of RhoC by inhibiting its geranylgeranylation provides an effective way to inhibit metastasis. Third, GGTIs may be useful to inhibit alternative prenylation of K-Ras4B.

GGTIs that specifically inhibit K-Ras4B geranylgeranylation but do not inhibit geranylgeranylation of RhoA are of interest, as they may provide a way to overcome one of the major shortcomings of currently available FTIs. While FTIs can potently inhibit FTase, they are incapable of inhibiting K-Ras, as this protein undergoes modification by GGTase I. See Tamanoi, F., Gau, C. L., Edamatsu, H., Jiang, C. and Kato-Stankiewicz, J. (2001) Protein farnesylation in mammalian cells, Cell Mol. Life Sci. 58, 1-14. The combined use of FTI and GGTI as well as the use of dual specificity FTIs that could inhibit both FTase and GGTase I has been attempted. See Lobell, R. B., Liu, D., Buser, C. A., Davide, J. P., DePuy, E., Hamilton, K., Koblan, K. S., Lee, Y., Mosser, S., Motzel, S. L., Abbruzzese, J. L., Fuchs, C. S., Rowinsky, E. K., Rubin, E. H., Sharma, S., Deutsch, P. J., Mazina, K. E., Morrison, B. W., Wildonger, L., Yao, S. L. and Kohl, N. E. (2002) Preclinical and clinical pharmacodynamic assessment of L-778,123, a dual inhibitor of farnesyl:protein transferase and geranylgeranyl:protein transferase type-I. Mol. Cancer Ther. 1, 747-758. Generation of GGTIs with specificity against K-Ras4B may inhibit K-Ras function without affecting other geranylgeranylated proteins. Such substrate specific GGTIs could then be combined with FTIs to inhibit all H, N, K-Ras proteins.

Chemical Definitions

Unless specified otherwise, the following chemical definitions are used throughout the sections below.

As used herein, the term “alkyl” denotes branched or unbranched hydrocarbon chains, preferably having about 1 to about 8 carbons, such as, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, 2-methylpentyl pentyl, hexyl, isohexyl, heptyl, 4,4-dimethyl pentyl, octyl, 2,2,4-trimethylpentyl and the like. “Substituted alkyl” includes an alkyl group optionally substituted with one or more functional groups which may be attached to such chains, such as, hydroxyl, bromo, fluoro, chloro, iodo, mercapto or thio, cyano, alkylthio, heterocyclyl, aryl, heteroaryl, carboxyl, carbalkoyl, alkyl, alkenyl, nitro, amino, alkoxyl, amido, and the like to form alkyl groups such as trifluoro methyl, 3-hydroxyhexyl, 2-carboxypropyl, 2-fluoroethyl, carboxymethyl, cyanobutyl and the like. “Bulky alkyl” includes cycloalkyl and branched chain alkyls with 4-8 carbons.

The term “cycloalkyl” as employed herein alone or as part of another group includes saturated or partially unsaturated (containing 1 or more double bonds) cyclic hydrocarbon groups containing 1 to 3 rings, including monocyclicalkyl, bicyclicalkyl and tricyclicalkyl, containing a total of 3 to 20 carbons forming the rings, preferably 3 to 10 carbons, forming the ring and which may be fused to 1 or 2 aromatic rings as described for aryl, which include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl and cyclododecyl, cyclohexenyl. “Substituted cycloalkyl” includes a cycloalkyl group optionally substituted with 1 or more substituents such as halogen, alkyl, alkoxy, hydroxy, aryl, aryloxy, arylalkyl, cycloalkyl, alkylamido, alkanoylamino, oxo, acyl, arylcarbonylamino, amino, nitro, cyano, thiol and/or alkylthio and/or any of the substituents included in the definition of “substituted alkyl.” For example,

and the like.

Unless otherwise indicated, the term “alkenyl” as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 2 to 12 carbons, and more preferably 2 to 8 carbons in the normal chain, which include one or more double bonds in the normal chain, such as vinyl, 2-propenyl, 3-butenyl, 2-butenyl, 4-pentenyl, 3-pentenyl, 2-hexenyl, 3-hexenyl, 2-heptenyl, 3-heptenyl, 4-heptenyl, 3-octenyl, 3-nonenyl, 4-decenyl, 3-undecenyl, 4-dodecenyl, 4,8,12-tetradecatrienyl, and the like. “Substituted alkenyl” includes an alkenyl group optionally substituted with one or more substituents, such as the substituents included above in the definition of “substituted alkyl” and “substituted cycloalkyl.”

The term “alkynyl” as used herein by itself or as part of another group refers to straight or branched chain radicals of 2 to 20 carbons, preferably 2 to 12 carbons and more preferably 2 to 8 carbons in the normal chain, which include one or more triple bonds in the normal chain, such as 2-propynyl, 3-butynyl, 2-butynyl, 4-pentynyl, 3-pentynyl, 2-hexynyl, 3-hexynyl, 2-heptynyl, 3-heptynyl, 4-heptynyl, 3-octynyl, 3-nonynyl, 4-decynyl, 3-undecynyl, 4-dodecynyl and the like. “Substituted alkynyl” includes an alkynyl group optionally substituted with one or more substituents, such as the substituents included above in the definition of “substituted alkyl” and “substituted cycloalkyl.”

The terms “arylalkyl”, “arylalkenyl” and “arylalkynyl” as used alone or as part of another group refer to alkyl, alkenyl and alkynyl groups as described above having an aryl substituent. Representative examples of arylalkyl include, but are not limited to, benzyl, 2-phenylethyl, 3-phenylpropyl, phenethyl, benzhydryl and naphthylmethyl and the like. “Substituted arylalkyl” includes arylalkyl groups wherein the aryl portion is optionally substituted with one or more substituents, such as the substituents included above in the definition of “substituted alkyl” and “substituted cycloalkyl.”

The terms “arylalkyl”, “arylalkenyl” and “arylalkynyl” as used alone or as part of another group refer to alkyl, alkenyl and alkynyl groups as described above having an aryl substituent. Representative examples of arylalkyl include, but are not limited to, benzyl, 2-phenylethyl, 3-phenylpropyl, phenethyl, benzhydryl and naphthylmethyl and the like. “Substituted arylalkyl” includes arylalkyl groups wherein the aryl portion is optionally substituted with one or more substituents, such as the substituents included above in the definition of “substituted alkyl” and “substituted cycloalkyl.”

The term “halogen” or “halo” as used herein alone or as part of another group refers to chlorine, bromine, fluorine, and iodine.

The terms “halogenated alkyl”, “halogenated alkenyl” and “alkynyl” as used herein alone or as part of another group refers to “alkyl”, “alkenyl” and “alkynyl” which are substituted by one or more atoms selected from fluorine, chlorine, bromine, fluorine, and iodine.

The term “aryl” or “Ar” as employed herein alone or as part of another group refers to monocyclic and polycyclic aromatic groups containing 6 to 10 carbons in the ring portion (such as phenyl or naphthyl including 1-naphthyl and 2-naphthyl) and may optionally include one to three additional rings fused to a carbocyclic ring or a heterocyclic ring (such as aryl, cycloalkyl, heteroaryl or cycloheteroalkyl rings).

“Substituted aryl” includes an aryl group optionally substituted with one or more functional groups, such as halo, haloalkyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, trifluoromethyl, trifluoromethoxy, alkynyl, cycloalkyl-alkyl, cycloheteroalkyl, cycloheteroalkylalkyl, aryl, heteroaryl, arylalkyl, aryloxy, aryloxyalkyl, arylalkoxy, alkoxycarbonyl, arylcarbonyl, arylalkenyl, aminocarbonylaryl, arylthio, arylsulfinyl, arylazo, heteroarylalkyl, heteroarylalkenyl, heteroarylheteroaryl, heteroaryloxy, hydroxy, nitro, cyano, amino, substituted amino wherein the amino includes 1 or 2 substituents (which are alkyl, aryl or any of the other aryl compounds mentioned in the definitions), thiol, alkylthio, arylthio, heteroarylthio, arylthioalkyl, alkoxyarylthio, alkylcarbonyl, arylcarbonyl, alkylaminocarbonyl, arylaminocarbonyl, alkoxycarbonyl, aminocarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfinylalkyl, arylsulfonylamino or arylsulfonaminocarbonyl and/or any of the alkyl substituents set out herein.

The term “heterocyclic” or “heterocycle”, as used herein, represents an unsubstituted or substituted stable 5- to 10-membered monocyclic ring system which may be saturated or unsaturated, and which consists of carbon atoms and from one to four heteroatoms selected from N, O or S, and wherein the nitrogen and sulfur heteroatoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized. The heterocyclic ring may be attached at any heteroatom or carbon atom which results in the creation of a stable structure. Examples of such heterocyclic groups include, but is not limited to, piperidinyl, piperazinyl, oxopiperazinyl, oxopiperidinyl, oxopyrrolidinyl, oxoazepinyl, azepinyl, pyrrolyl, pyrrolidinyl, furanyl, thienyl, pyrazolyl, pyrazolidinyl, imidazolyl, imidazolinyl, imidazolidinyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isooxazolyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, thiadiazolyl, tetrahydropyranyl, thiamorpholinyl, thiamorpholinyl sulfoxide, thiamorpholinyl sulfone, and oxadiazolyl. The term “heterocyclic aromatic” as used here in alone or as part of another group refers to a 5- or 7-membered aromatic ring which includes 1, 2, 3 or 4 hetero atoms such as nitrogen, oxygen or sulfur and such rings fused to an aryl, cycloalkyl, heteroaryl or heterocycloalkyl ring (e.g. benzothiophenyl, indolyl), and includes possible N-oxides. “Substituted heteroaryl” includes a heteroaryl group optionally substituted with 1 to 4 substituents, such as the substituents included above in the definition of “substituted alkyl” and “substituted cycloalkyl.” Examples of heteroaryl groups include the following:

and the like.

I. Pilot Library Construction and Screening

To overcome the problems associated with the diversity-oriented synthesis, an approach was developed that employs allenoates as multireactive core molecule and uses another set of building blocks (imines, aldehydes and maleimides) that react with allenoates under similar reaction conditions (phosphine catalysis). This led to the production of diverse compounds including dihydropyrroles and tetrahydropyridines.

A pilot library was constructed using allenoate as a multireactive core molecule. This pilot library was screened for compounds which inhibited protein farnesyltransferase (FTase), that is, farnesyltransferase inhibitors (FTIs), and for compounds which inhibited protein geranylgeranyltransferase type I (GGTase I), that is geranylgeranyltransferase type I inhibitors (GGTIs). Because these enzymes catalyze modification of signaling proteins such as Ras, Rheb and Rho, small molecule inhibitors can be anti-cancer therapeutics. 4,314 compounds were synthesized and screened for compounds with improved potency of inhibition. As discussed further below, structure activity relationship studies of these compounds pointed to the significance of certain substitution patterns on the aromatic substitutions of the scaffold ring structure of initial hits.

Construction of a Pilot Library Based on Allenoate Chemistry

The pilot library was constructed by reacting allenoates with imines, aldehydes and maleimides under phosphine catalysis conditions to produce an array of compounds including dihydropyrroles, tetrahydropyridines, bicyclic succinimides, dioxanylidenes and dihydrofurans. The 171 compounds produced for the pilot library are illustrated in FIG. 1.

Identification of Novel Inhibitors of Protein Geranylgeranyltransferase Type I

The pilot library was screened for inhibitors of protein geranylgeranyltransferase type I. Protein prenyltransferase assays were carried out by using filter binding. Two different substrates, RhoA and K-Ras4B, were used for the assay. RhoA ends with the CaaL motif and is an exclusive substrate for GGTase I, while K-Ras4B ends with the CaaX motif and is modified by both GGTase I and FTase. The presence of a polybasic domain consisting of a stretch of lysine close to the CaaX motif enables this CaaX motif to be recognized by GGTase I. Thus, RhoA and K-Ras4B are two very different substrates of this enzyme and it is of interest to identify small molecule inhibitors exhibiting preferential inhibition on reaction driven by one substrate over another.

Screening of the 171-compound pilot library resulted in the identification of three groups of compounds shown in FIG. 2. In the assay, a fixed concentration of 100 μM was used and the results are plotted for the inhibition of RhoA (vertical axis) as well as for K-Ras4B (horizontal axis). A group of compounds that contain P2-D5, P2-D7, P2-D8, P2-D9 and P2-D10 inhibit GGTase I equally when using RhoA and K-Ras4B as substrates. They are 2,6-diaryl-N-tosyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids, except P2-D5 that is missing an aryl substituent at C2. The second group of compounds, P2-F10, P2-F12, P2-G3 and P2-G6, exhibits somewhat stronger inhibition when using K-Ras4B as a substrate. In particular, P2-F10 demonstrates significant inhibition of GGTase I when K-Ras4B is used as a substrate, while virtually no inhibition was observed when RhoA was used as a substrate. It is worth pointing out that known GGTI compound GGTI-298 and GGTI-2166 inhibit RhoA-driven GGTase I activity slightly better than K-Ras4B-driven GGTase I activity (FIG. 17). This group of compounds possesses 5-alkyl-2-aryl-N-tosy-2,5-dihydropyrrole-3-carboxylic acid structure, which is distinct from the previously described tetrahydropyridine motif.

Another compound that is different from the above two groups was also identified. This compound, labeled P1-F10, inhibited GGTase-I when using RhoA as a substrate but virtually no inhibition was seen when K-Ras4B was used as a substrate. The GGTIs identified did not inhibit FTase at the same concentration.

It has been reported that some chemical compounds form aggregates at high concentrations and that these aggregates inhibit a variety of enzyme reactions. See (a) McGovern, S. L., Caselli, E., Grigorieff, N. and Shoichet, B. K. (2003) A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening. J. Med. Chem. 45, 1712-1722. (b) McGovern, S. L., Helfand, B. T., Feng, B. and Shoichet, B. K. (2003) A specific mechanism of nonspecific inhibition. J. Med. Chem. 46, 4265-4272. To exclude this possibility, one can add a detergent that can prevent formation of these aggregates. As can be seen in FIG. 3, the inhibition of GGTase I observed was unaffected by the presence of the detergent (0.01% TritonX-100). Similarly, all the inhibitions observed could be reproduced in the presence of the detergent.

Identification of Novel Inhibitors of Protein Farnesyltransferase

To further characterize the pilot library, inhibitors of protein farnesyltransferase were identified. This was accomplished by using K-Ras4B as a substrate protein, tritiated farnesylpyrophosphate ([³H]FPP) and protein farnesyltransferase. See Finegold, A. A., Johnson, D. I., Farnsworth, C. C., Gelb, M. H., Judd, S. R., Glomset, J. A. and Tamanoi, F. (1991) Protein geranylgeranyltransferase of Saccharomyces cerevisiae is specific for Cys-Xaa-Xaa-Leu motif and requires the CDC43 gene product but not the DPRI gene product. Proc. Natl. Acad. Sci. USA 88, 4448-4452. This screen led to the identification of six hit compounds shown in FIG. 4. Interestingly, compounds P1-E11, P1-F1 and P1-F2 contain a common structure that is distinct from those identified as GGTI compounds above. On the other hand, the structure of the compounds P1-F11, P2-B7 and P2-E9 resemble those of GGTIs. The FTI P1-F11 resembles the GGTI P1-F10, while the FTI P2-B7 resembles the GGTI P2-C10. The FTI P2-E9 is similar to the GGTI P2-G3. Similarity of some GGTI and FTI compounds may point to common structural features between the two closely related enzymes. As described before, FTase and GGTase I have similar three-dimensional structures and a shared alpha subunit. On the other hand, FTase specific inhibitors may recognize a region(s) that is different between the two enzymes. The FTIs identified here exhibit a weaker inhibition of GGTase I at the concentration that inhibits FTase.

Further Diversification of the Compound Library and Identification of Improved GGTI Compounds

An advantage of using the diversity oriented library described herein is that it is possible to quickly synthesize a large number of compounds that are related to lead compounds. Split-and-pool synthesis on solid support is one of the fastest and most efficient ways of generating a large number of spatially segregated compounds. See (a) Furka, A.; Sebestyen, F.; Asgedom, M.; Dibó (1988), in Highlights of Modern Biochemistry, Proceedings of the 14th International Congress of Biochemistry. Prague. Czechoslovakia (VSP, Utrecht, Netherlands), 13, 47. (b) Furka, A.; Sebestyen, F.; Asgedom, M.; Dibó (1991), Int. J. Pept. Protein Res. 37, 487. (c) Houghton, R. A.; Pinilla, C.; Blondelle, S. E.; Appel, J. R.; Dooley, C. T.; Cuervo, J. H. (1991) “Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery” Nature 354, 84-86. (d) Lam, K. S.; Salmon, S. E.; Hersh, E. M.; Hruby, V. J.; Kazmierski, W. M.; Knapp, R. J. (1991) “A new type of synthetic peptide library for identifying ligand-binding activity” Nature 354, 82-84.; (e) Obrecht, D.; Villalgordo, J. M. (1998) Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries, Elsevier Science Ltd, Oxford. Use of the IRORI NanoKan system or SynPhase™ Lanterns alleviates the need for chemical encoding, and provides more material for a given compound than using beads. More information on these systems may be found at www.discoverypartners.com/products/irori_tech_nanokan.html or www.synphase.com/combichem/lanterns.html. It was decided to use SynPhase Lanterns but as one of skill in the art will appreciate the invention described herein is not limited to using SynPhase Lanterns (available from Mimotopes Pty Ltd., Victoria, Australia).

The SynPhase Lantern consists of a grafted mobile surface polymer (such as polystyrene) onto a rigid and unreactive base polymer that is cylindrical in appearance. The SynPhase Lantern is available in three different sizes, with loadings of 15 μmol, 35 μmol, and 75 μmol. Considering that a typical assay requires 1 nmol of a small organic molecule, 15˜75 μmol of compound provides a large enough quantity of chemicals for multiple assays. The rigid polymeric support of lanterns beneath a grafted mobile phase makes weighing unnecessary and handling easier than with resins.

The overall reaction sequence for this diversification to 4,314 compounds is schematized in FIG. 5. Validation of the synthetic route on polymer support commenced with formation of resin-bound allenoates 2 and 3. In optimum loading procedures, allenoic acids were coupled with the benzyl alcohol of the SynPhase-PS Lanterns grafted with Wang resin 1 by using Mukaiyama's reagent. See (a) Mukaiyama, T.; Usui, M.; Shimada, E.; Saigo, K. (1975) “A Convenient Method for the Synthesis of Carboxylic Esters” Chem. Lett. 1045-1048. (b) Mukaiyama, T.; Toda, H.; Kobayashi, S. (1976) “Betaine as an Effective Acid Captor: A Convenient Method for the Synthesis of Carboxylic Esters” Chem. Lett. 13-14. (c) Saigo, K.; Usui, M.; Kikuchi, K.; Shimada, E.; Mukaiyama, T. (1977) “New Method for the Preparation of Carboxylix Esters” Bull. Chem. Soc. Jpn. 50, 1863-1866. The phosphine-catalyzed annulation between polymer-supported allenoates 2 and 3 and N-sulfonyl-arylimine proceeded smoothly to provide polymer-bound dihydropyrroles 4 and tetrahydropyridines 5. Heterocycles 4 and 5 were cleaved off the resin in order to furnish acids 6 and 7 in 91˜92% yield (based on a theoretical loading of 15 □M/Lantern) after flash column chromatography (FCC). The Michael addition of thiols to 4 and 5 with n-butyl lithium as a base provided 8 and 9, which, upon trifluoroacetic acid (TFA)-mediated cleavage, provided 10 and 11. See Miyata, O.; Shinada, T.; Ninomiya, I.; Naito, T.; Date, T.; Okamura, K.; Inagaki, S. (1991) “Stereospecific Nucleophilic Addition Reactions to Olefins. Addition of Thiols to α,β-Unsaturated Carboxylic Acid Derivatives” J. Org. Chem. 56, 6556-6564. The relative stereochemistry of 10 and 11 Was confirmed by X-ray crystallographic analysis. A Tebbe reaction on 5 furnished solid-bound enol ether 12 which could be cleaved from the polymer support under the influence of hydrochloric acid (HCl) to afford 0.13 in a 92% overall yield. See (a) Ball, C. P.; Barrett, A. G. M.; Commercon, A.; Compere, D.; Kuhn, C.; Roberts, R. S.; Smith, M. L.; Venier, O. (1998) “Chameleon Catches in Combinatorial Chemistry Tebbe Olefination of Polymer Supported Esters and the Synthesis of Amines, Cyclohexanones, Enones, Methyl Ketones and Thiazoles” Chem. Commun. 2019-2020. (b) Barrett, A. G. M.; Procopiou, p. A.; Voigtmann, U. (2001) “Solid-Phase Synthesis of Isoxazoles Using Vinyl Ethers as Chamelon Catches” Org. Lett. 3, 3165-3168; (d) Mori, A.; Yamamoto, H. (1985) “Resolution of Ketones via Chiral Acetals. Kinetic Approach” J. Org. Chem., 50, 5444-5446; (e) Lienhard, G. E.; Wang, T. (1969) “On the Mechanism of Acid-Catalyzed Enolization of Ketones” J. Am. Chem. Soc. 91, 1146-1153.

After the reaction routes to synthesize analogs of the GGTI hits were validated on solid support (see 6 and 7 in FIG. 5), we purchased/made the building blocks. The chemical reactions involved in building block preparation are as follows (FIG. 6). γ-substituted allenoic acid 17 was derived from the corresponding 7-substituted allenoate 16, which in turn was made by the reaction between phosphorane 14 and acid chloride 15. See Lang, R. W.; Hansen, H.-J. (1990) “α-Allenic Esters from α-Phosphoranylidene Esters and Acid Chlorides: Ethyl 2,3-Pentadienoate” Org. Synth. Coll. Vol. 7, 232-235. When phosphorane 14 was treated with alkyl halide 18, phosphonium halide 19 was obtained. Phosphonium halide 19 was converted to α-substituted allenoate 20 upon treatment with triethylamine (2 equiv) and acetyl chloride (1 equiv). See Scholz, D.; Weber-Roth, S.; Macoratti, E.; Francotte, E. (1999) “Expedient Synthesis of α-substituted α,β-unsaturated γ-amino acids (dipeptide memetics); Wittig reaction of α-amino aldehydes with α-substituted alkoxycarbonylphosphoranes” Synth. Commun. 29, 1143-1155.

α-substituted allenoic acid 21 was prepared by saponification of ester 20. N-sulfonylimine 24 was formed by the azeotropic removal of water from a refluxing toluene mixture of appropriate sulfonamide 22, aldehyde 23, and catalytic acid. See (a) McKay, W. R.; Proctor, G. R. (1981) “Removal of toluene-p-sulfonyl groups from sulfonamides. Part 4. Synthesis of phenylglyoxal imine monomers” J. Chem. Soc. Perkin Trans. 1, 2435-2442. (b) Jennings, W. B.; Lovely, C. J. (1991) “The titanium tetrachloride induced synthesis of N-phosphinoylimines and N-sulfonylimines directly from aromatic aldehydes” Tetrahedron, 47, 5561-5568. (c) Love, B. E.; Raje, P. S.; Williams II, T. C. (1994) “Preparation of N-Tosylaldimines” Synlett 493-494. (d) Bilodeau, M. T.; Cunningham, A. M. (1998) “Solid-Supported Synthesis of Imidazoles: A strategy for Direct Resin-Attachment to the Imidazole Core” J. Org. Chem. 63, 2800-2801. (e) Chemla, F.; Hebbe, V.; Normant, J.-F. (2000) “An Easy Synthesis of Aliphatic and Aromatic N-Sulfonyl Aldimines” Synthesis, 75-77.

The building blocks synthesized as illustrated in FIG. 6 are shown in FIG. 7 (γ-substituted allenoic acid 17), FIG. 8 (α-substituted allenoic acid 21), and FIG. 9 (N-sulfonylimine 24). The other building blocks, thiols, which were purchased for the library synthesis, are shown in FIG. 10.

Once the building blocks were synthesized, they were tested to determine whether or not they would be incorporated into the synthesis of the focused library of GGTIs. Building blocks were chosen so that only the ones that provided high purity (by ¹H NMR and LC/MS analysis) for the final crude products would be used in the synthesis of the library. The building blocks chosen for the synthesis of the library and the resulting number of compounds are shown in FIG. 11. Scaffolds that require distinctive set of reaction conditions are drawn separately.

For the synthesis of 2-aryl-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acid (6 with R1=H) 30 imines (C01-C03, C06, C09-C16, C18, C19, C23, C24, C26-C31, C33, C36, C40-C44, C46) provided satisfactory results to give 302-aryl-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acids (FIG. 11A).

For the synthesis of 5-alkyl-2-aryl-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acid 6 10 allenoic acids (A02-A11) and 21 imines (C01-C03, C06, C09-C14, C16, C20, C23, C24, C26, C27, C29, C30, C33, C40, C41) were selected to furnish 210 (10×21) 5-alkyl-2-aryl-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acids (FIG. 11B).

For 5-alkyl-2-aryl-4-mercapto-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acid 10 7 allenoic acids (A05-A11), 25 imines (C01-006, C09-C14, C16, C20, C21, C23, C24, C26, C27, C29, C30, C33, C35, C40, C41), and 19 thiols (E01, E02, E04, E06, E07, E16-E25, E28-E30, E32) were chosen to give 3,325 (7×25×19) 5-alkyl-2-aryl-4-mercapto-N-sulfonyl-2,5-dihydropyrrole-3-carboxylic acids (FIG. 11C).

For 6-aryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acid 7 (with R3=H) 26 imines (C01-C06, C10, C12, C15, C16, C20, C21, C24, C25, C30, C33-C43) were selected resulting in 266-aryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids (FIG. 11D).

For 3-acyl-6-aryl-N-sulfonyl-1,2,5,6-tetrahydropyridine 13 25 imines (C01-C06, C10-C12, C15, C16, C20, C21, C24, C25, C30, C33-C43, C46) provided satisfactory results to give 25 3-acyl-6-aryl-N-sulfonyl-1,2,5,6-tetrahydropyridines (FIG. 11E).

For 2,6-diaryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acid 7 11 □-substituted allenoic acids (B02-B12) and 31 imines (C01-006, C09-C13, C15, C19-C21, C23, C24, C26-C28, C30, C33, C35, C37-C43, C46) were selected resulting in 341 (11×31) 2,6-diaryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids (FIG. 11F).

For 6-aryl-4-mercapto-N-sulfonyl-piperidine-3-carboxylic acid 11 21 imines (C01-006, C10-C12, C15, C20, C25, C30, C35, C37-C41, C43, C46) and 17 thiols (E01, E02, E04-E07, E09, E15, E16, E18, E21-E25, E28, E30) were chosen to provide 357 (21×17) 6-aryl-4-mercapto-N-sulfonyl-piperidine-3-carboxylic acids (FIG. 11G). The total number of compounds for the library is, therefore, 4,314 compounds.

The next step was the split-and-pool synthesis of a library of heterocycles (shown in FIG. 5). The first split step of the proposed library synthesis is the coupling of 23 different allenoic acids to the benzyl alcohol of the Wang resin. In the second split step, resin-bound allenoates (MCMs) react with imines under nucleophilic phosphine catalysis conditions to generate two distinctive heterocycles 4 and 5. The last split step involves use of the α,β-unsaturated ester moiety (MCF) in stereoselective Michael addition using thiols to further increase structural diversity, resulting in two additional scaffolds 8 and 9. 240 Lanterns with resin-bound heterocycle 4, 357 with 5, 3,325 with 8, and 357 with 9 were inserted in individual vials and cleaved with 2.5% TFA in methylene chloride to provide the corresponding carboxylic acids. 25 Lanterns with polymer-bound heterocycle 5 were treated with Tebbe reagent to afford enol ether 12, which was cleaved with 0.1 N HCl in acetone to give 25 enones 13. Use of resin-bound allenoates facilitated solid-phase combinatorial synthesis of heterocyclic compounds in a split-and-pool fashion. Use of SynPhase™ Lanterns alleviated the need for chemical encoding and provide more material for a given compound. See (a) Gerritz, S. W.; Norman, M. H.; Barger, L. A.; Berman, J.; Bigham, E. C.; Bishop, M. J.; Drewry, D. H.; Garrison, D. T.; Heyer, D.; Hodson, S. J.; Kakel, J. A.; Linn, J. A.; Marron, B. E.; Nanthakumar, S. S.; Navas, F. J., III. (2003) “High-Throughput Manual Parallel Synthesis Using SynPhase Crowns and Lanterns” J. Comb. Chem. 5, 110-117. (b) Feliu, L.; Subra, G.; Martinez, J.; Amblard, M. (2003) “Spiroimidazolidinone Library Derivatives on SynPhase Lanterns” J. Comb. Chem. 5, 356-361. L-series lanterns of 15 μmol loading were used for our library synthesis. The identity of the building blocks used in the synthesis of the individual members of the library was encoded by colored spindles and cogs.

With 4,314 small molecules in hand, their inhibitory activity against GGTase I for K-Ras4B and RhoA was examined. All members of the library that contain tetrahydropyridine and piperidine scaffolds were screened. These members correspond to 749 compounds of 7, 11, and 13. The GGTI compounds exhibiting over 80% inhibition of GGTase activity at 50 μM concentration are shown in FIGS. 12, 13 and 14. The first compartment of each table contains the structure of a representative scaffold. The first row and the first column of each table list building blocks used to make GGTI compounds shown in the table. A pair of numbers below the structure of a GGTI is % activities of GGTase I for proteins K-Ras4B/RhoA in the presence of the GGTI compound. Smaller numbers indicate better inhibition. Activities below 10% (over 90% inhibition) for both proteins are underlined. Significantly better inhibition for RhoA over K-Ras4B is in parenthesis.

2,6-Diaryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids 7 that contain 10α-substituted allenoic acids (in the order of frequency of appearance: B06>B05>B07>B04=B02=B10>B03=B08=B09=B11) and 7 imines (C40>C13>C15>C12=C27>C30=C24) showed prominent inhibitory activities (FIG. 12).

For the measured inhibitory activities of individual compounds, see FIGS. 19-1 through 19-27. The “label” column provides annotation (e.g., B01C01T means a compound made of B01 and C01 and the Tebbe reaction, and B01C01E21 means a compound made of building blocks B01, C01, and E21) of each compound for each entry. The “Kras” column provides % activity of GGTase I for protein K-Ras4B in the presence of the compound of that entry.

The % activity of GGTase I was determined as follows: a working solution that contained each compound in DMSO at the concentration of 1 mM was prepared. The working solution was added to GGTase I reaction mixture so that the final concentration of the compound is 50 μM. GGTase I activity was assayed by incubating [³H]GGPP with K-Ras4B or RhoA protein in the presence of GGTase I and examining radioactivity incorporated into the substrate protein by spotting onto a filter paper. After washing with TCA, ethanol and acetone, the radioactivity retained on the filter was determined by the use of a scintillation counter. GGTase I activity in the presence of DMSO was taken as a 100% value and the activity in the presence of the compound was shown as percent activity compared with the 100% value. The table in FIG. 12 shows 24 2,6-diaryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids 7 that were selected out of 367 compounds. None of the enones 13 were active indicating that the carboxylic acid moiety is crucial for the GGTI activity. For 6-aryl-4-mercapto-N-sulfonyl-piperidine-3-carboxylic acid 11 the 4-mercapto substituent appeared critical to endowing GGTase inhibitory activity. 16 compounds out of 21 possessing 4-phenethylthio moiety (E15) were active (FIG. 13). 4-Chlorobenzylthio substituent was the next best; 12 compounds out of 21 containing the 4-chlorobenzylthio moiety were active. 4-Benzylthio substituent was also good; 7 piperidines out of 21 bearing 4-benzylthio group were active. Less frequently appearing 4-mercapto substituents are summarized in FIG. 14. Nine thiols (E15>E09>E06 >>E22>E05=E23=E21=E30>E24) out of 17 thiols showed up in the GGTIs. 19 imines (C15>C12=C41>C40>C01=C11>C05=C10=C30=C35=C37=C38>C02, C03, C04, C06, C39=C43) out of 21 appeared in the GGTIs. 4 Imines, C15, C12, C41 and C40, are particularly interesting since they showed up in more than three GGTI compounds. This corresponds to 47 6-aryl-4-mercapto-N-sulfonyl-piperidine-3-carboxylic acids out of 357 compounds. These 71 GGTIs exhibited better inhibition for RhoA over K-Ras4B; some with 100 fold stronger inhibitory activity for RhoA over K-Ras4B (e.g., compound P4-G5=B01C15E05).

Dose dependency of the inhibition of two compounds is shown in FIG. 15. IC50 values for the inhibition of GGTase I using RhoA as a substrate were 5 and 7 □M for P3-D9 and P3-E5, respectively (see FIG. 12 for the structures of P3-D9 and P3-E5). Under the same reaction condition, IC50 values of 1.6 and 0.5 □M were determined for the known GGTIs, GGTI-298 and GGTI-2166, respectively. Specificity of GGTase I inhibition by P3-D9 and P3-E5 was examined. As can be seen in FIG. 16, no inhibition of FTase activity was observed by these compounds even when the concentration was increased to 100 μM. FTI compound (BMS225975) used as a control inhibits FTase but does not inhibit GGTase I. GGTI-298 inhibits GGTase I while little inhibition was observed with FTase (see FIG. 17 for the structures of P5-H6 and GGTI-298).

Identification of Substrate Specific GGTI Compounds

Our screening also led to the identification of compounds that exhibit preferential inhibition of GGTase using a particular substrate. FIG. 17 lists GGTI compounds with reproducibly stronger inhibition of K-Ras4B driven GGTase I over RhoA driven activity. For example, the novel compound P4-F1 inhibits K-Ras4B driven GGTase I activity, but does not inhibit RhoA-driven GGTase I activity.

Analysis of the structures in FIG. 12 suggest construction of a library of 2,6-diaryl-N-sulfonyl-1,2,5,6-tetrahydropyridine-3-carboxylic acids 7 consisting of B02 through B07 and new imines C47 through C49 for further improvement of GGTI activity (FIG. 18). Perusal of the GGTI compounds in FIGS. 13 and 14 indicated a library of 6-aryl-4-mercapto-N-sulfonyl-piperidine-3-carboxylic acid 11 built with 801, new imines C47 through C51, and thiols (E15>E09>E06 >>E22>E05) would be the next step for further improvement of GGTI activity

II. GGTI Compounds

Through the library screening and other assays described herein, numerous compounds have been identified that can inhibit GGTase I. These compounds have the formula:

wherein J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen,

wherein G is

wherein E is selected from the group consisting of hydrogen, C₁-C₃ alkyl, and halogen,

wherein W is selected from the group consisting of cyclic, linear, or branched alkyl of from 2 to 8 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen,

wherein X—Y is selected from the group consisting of

wherein A is selected from the group consisting of

and —CO₂M;

wherein M is selected from the group consisting of hydrogen and alkyl of from 1 to 2 carbons,

wherein n is between 0 and 3 carbons;

wherein R is any alpha-substituent of an amino acid;

wherein Z is S—U; and

wherein U is selected from the group consisting of alkyl of from 2 to 10 carbons.

In some embodiments, these compounds may be based on scaffolds 6, 7, and 10. These scaffolds have the following structures:

The compounds constructed on scaffold 6 may include substituents at R1, P and R3. R1 may be selected from the group consisting of linear or branched alkyl of from 2 to 6 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen. In some embodiments, R1 is tert-butyl, cyclopentyl methyl, or another bulky alkyl or cycloalkyl group. R1 is represented herein as W as well.

In some embodiments, P is a protecting group. While many protecting groups may be used at P, the following protecting group is preferred:

P is also represented as G herein. In some embodiments, E is selected from the group consisting of hydrogen, C₁-C₃ alkyl, and halogen. In some embodiments, E is a methyl group.

R3 can be an unsubstituted phenyl or a substituted phenyl ring. The substitution (also represented as J) can be at any position on the phenyl ring. In some embodiments, J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen.

One embodiment of the compounds that may be built from scaffold 6 is compound UC-22 (also referred to as P5-H6). This compound has the following chemical structure:

Some exemplary compounds that inhibit GGTase I activity based on scaffold 6 include those listed in Table 1:

TABLE 1 Exemplary Compounds Based on Scaffold 6

C40 R³ = 4-chlorophenyl P = 2-methylbenzene- sulfonyl C26 R³ = 3-fluorophenyl P = 4-methylbenzene- sulfonyl C20 R³ = 3,4-dimethoxyphenyl P = 4-methylbenzene- sulfonyl A03 R¹ = tert-butyl

P5-H6 13.3/5.3

23.7/9.1

23.4/6.1 A11 R¹ = cyclopentylmethyl

23.7/9.1

Further compounds of interest that can be based on scaffold 6 are listed in FIG. 2. These compounds include P2-F10, P2-F12, P2-G3 and P2-G6.

In some embodiments, GGTase I inhibiting compounds can be based on scaffold 7. The compounds based on scaffold 7 may include substituents at R3, P and R2. R3 may be selected from the group consisting of linear or branched alkyl of from 2 to 6 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen. R3 is represented herein as W as well.

In some embodiments, P is a protecting group as described above.

R2 can be an unsubstituted phenyl or a substituted phenyl ring. The substitution (also represented as J) can be at any position on the phenyl ring. In some embodiments, J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen.

One embodiment of the compounds that may be based on scaffold 7 is compound UC-23 (also referred to as P3-E5). This compound has the following chemical structure:

Some exemplary compounds that inhibit GGTase I activity based on scaffold 7 include those listed in Table 2:

TABLE 2 Exemplary Compounds Based on Scaffold 7

7 K-ras/RhoA             C40 R³ = 4-chlorophenyl P = 2-methylbenzene- sulfonyl             C13 R³ = 3,4-dichlorophenyl P = 4-methylbenzene- sulfonyl B06 R² = 3-bromophenyl

10.6/8.8

8.6/3.2 B05 R² = 3-chlorophenyl

P3-E5 41.7/24.8 14.7/7.5

10.7/4.5 B07 R² = 3-methylphenyl

15.6/12.4

12.6/10.3 B04 R² = 3-fluorophenyl

5.4/3.0 B02 R² = phenyl

13.4/5.8 B10* R² = 4-bromophenyl

18.7/11.3 B03 R² = 2-fluorophenyl

8.4/4.1 B08 R² = 4-fluorophenyl

15.6/12.6 B09 R² = 4-chlorophenyl

17.7/12.1 B11 R² = 4-methylphenyl

12.4/15.6

7 K-ras/RhoA             C15 R³ = 3-bromophenyl P = 4-methylbenzene- sulfonyl             C12 R³ = 3-chlorophenyl P = 4-methylbenzene- sulfonyl B06 R² = 3-bromophenyl

9.4/3.7

11.0/7.0 B05 R² = 3-chlorophenyl

9.8/7.9

(43.7/6.0) B07 R² = 3-methylphenyl

16.1/14.3 B04 R² = 3-fluorophenyl

17.0/15.0 B02 R² = phenyl

35.2/19.4 B10* R² = 4-bromophenyl B03 R² = 2-fluorophenyl B08 R² = 4-fluorophenyl B09 R² = 4-chlorophenyl B11 R² = 4-methylphenyl

7 K-ras/RhoA             C27 R³ = 4-chlorophenyl P = 4-chlorobenzene- sulfonyl             C30 R³ = 4-methylphenyl P = 4-chlorobenzene- sulfonyl B06 R² = 3-bromophenyl

8.6/5.0

8.4/7.4 B05 R² = 3-chlorophenyl

P3-D9 33.1/26.7 B07 R² = 3-methylphenyl B04 R² = 3-fluorophenyl B02 R² = phenyl B10* R² = 4-bromophenyl B03 R² = fluorophenyl B08 R² = 4-fluorophenyl B09 R² = 4-chlorophenyl B11 R² = 4-methylphenyl

Further compounds of interest that can be based on scaffold 7 are listed in FIG. 2. These compounds include P2-D5, P2-D7, P2-D8, P2-D9, and P2-D10.

Other compounds may be built on scaffold 10. The compounds constructed on scaffold 10 may include substituents at R1, P, R3 and SR4 positions. R1 may be selected from the group consisting of is selected from the group consisting of linear or branched alkyl of from 1 to 6 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen. R1 is represented herein as W as well.

In some embodiments, P is a protecting group as described above.

R3 can be an unsubstituted phenyl or a substituted phenyl ring. The substitution (also represented as J) can be at any position on the phenyl ring. In some embodiments, J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen.

SR4 can be represented as thiols, with R4 being selected from the group consisting of hydrogen, alkyl of from 2 to 10 carbons.

Some exemplary compounds that inhibit GGTase I activity have been built using scaffold 10 include those listed in Table 3:

TABLE 3 Exemplary Compounds Based on Scaffold 10

10 K-ras/RhoA                 E30 R⁴ = allyl                 E32 R⁴ = 2-(tert-buthoxycarbonyl)ethyl                 E04 R⁴ = 4-methoxyphenyl C26 R³ = 3-fluorophenyl P = 4-methylbenzene- sulfonyl

30.4/9.7

20.2/7.8

27.4/3.5

31.9/8.2 C13 R³ = 3,4-dichlorophenyl P = 4-methylbenzene- sulfonyl

21.4/9.6

27.2/7.6

10.9/1.1

15.1/6.8

16.1/7.3

12.1/8.6 C40 R³ = 4-chlorophenyl P = 2-methylbenzene- sulfonyl

28.4/8.9

10.0/7.8

23.1/8.4

24.9/6.0

22.4/4.9 C27 R³ = 4-chlorophenyl P = 4-chlorobenzene- sulfonyl

21.7/9.2

48.7/8.0  

22.5/9.8 C29 R³ = 4-chlorophenyl P = benzenesulfonyl

30.4/9.7 C09 R³ = 4-cyanophenyl P = 4-methylbenzene- sulfonyl

23.1/9.3

21.5/6.0 C14 R³ = 4-bromophenyl P = 4-methylbenzene- sulfonyl

9.8/7.5

15.5/5.5 C12 R³ = 2-chlorophenyl P = 4-methylbenzene- sulfonyl

20.6/5.6

25.5/6.5 C20 R³ = 3,4-dimethoxyphenyl P = 4-methylbenzene- sulfonyl

22.3/8.1 C11 R³ = 4-chlorophenyl P = 4-methylbenzene- sulfonyl

25.2/7.7 C24 R³ = 4-isopropylphenyl P = 4-methylbenzene- sulfonyl

31.7/6.1

10 K-ras/RhoA                 E02 R⁴ = 4-methylphenyl         E23 R⁴ = 3-methyl-1-butyl or E24 R⁴ = pentyl or E28 R⁴ = cyclopentyl C26 R³ = 3-fluorophenyl P = 4-methylbenzene- sulfonyl

14.7/4.1

23.5/7.1

31.5/7.1 C13 R³ = 3,4-dichlorophenyl P = 4-methylbenzene- sulfonyl

21.3/9.2 C40 R³ = 4-chlorophenyl P = 2-methylbenzene- sulfonyl C27 R³ = 4-chlorophenyl P = 4-chlorobenzene- sulfonyl C29 R³ = 4-chlorophenyl P = benzenesulfonyl

15.0/7.5

28.1/5.9 C09 R³ = 4-cyanophenyl P = 4-methylbenzene- sulfonyl

20.1/7.4 C14 R³ = 4-bromophenyl P = 4-methylbenzene- sulfonyl C12 R³ = 2-chlorophenyl P = 4-methylbenzene- sulfonyl C20 R³ = 3,4-dimethoxyphenyl P = 4-methylbenzene- sulfonyl C11 R³ = 4-chlorophenyl P = 4-methylbenzene- sulfonyl C24 R³ = 4-isopropylphenyl P = 4-methylbenzene- sulfonyl

The compounds based on the scaffolds listed herein may be prepared, for example, using the synthesis method illustrated in FIG. 6. However, as one of skill in the art will appreciate, other synthesis methods may be used and the invention is not limited to the method illustrated in FIG. 6.

Other compounds, including exemplary compound mP5-H6, can be prepared using the following synthesis method:

Compound mP5-H6 has been prepared using this synthesis method. Compound mP5-H6 has the structure depicted in the above synthesis method and exhibits the GGTase I inhibiting activity shown in the examples below.

Other compounds can be prepared using the methods described herein. In some embodiments, these compounds have the following chemical structure:

While n is depicted as 1-3, in some embodiments n can be 0. In other embodiments, n is 1, 2, or 3.

The compounds herein may be made using the synthetic methods described herein. One of skill in the art will appreciate that the various substituent groups depicted and described as part of the library can be added to each scaffold to produce compounds that fall within the scope of the present invention. For example, the substituent groups illustrated in Tables 1, 2, and 3 may be placed on scaffold 6, 7, or 10 regardless of whether the substituent group is depicted on that scaffold herein.

As one of skill in the art will appreciate, the compounds described herein may be used in a salt form (e.g., a sodium, potassium, or other pharmaceutically acceptable salt) or in a crystalline form. For some compounds, e.g., mP5-H6, a salt cannot be readily prepared using conventional methods but, as one of skill in the art will appreciate, alternative methods may be used to prepare a salt. The salt or crystalline forms of the compounds described herein may be useful as part of a pharmaceutical composition.

Pharmaceutical Compositions

The compounds of the invention are useful as pharmaceutical compositions prepared with a therapeutically effective amount of a compound of the invention, as defined herein, and a pharmaceutically acceptable carrier or diluent.

The compounds of the invention can be formulated as pharmaceutical compositions and administered to a subject in need of treatment, for example a mammal, such as a human patient, in a variety of forms adapted to the chosen route of administration, for example, orally, nasally, intraperitoneally, or parenterally, by intravenous, intramuscular, topical or subcutaneous routes, or by injection into tissue.

Suitable oral forms for administering the compounds include, lozenges, troches, tablets, capsules, effervescent tablets, orally disintegrating tablets, floating tablets designed to increase gastric retention times, buccal patches, and sublingual tablets.

The compounds of the invention may be systemically administered, e.g., orally, in combination with a pharmaceutically acceptable vehicle such as an inert diluent or an assimilable edible carrier, or by inhalation or insufflation. They may be enclosed in coated or uncoated hard or soft shell gelatin capsules, may be compressed into tablets, or may be incorporated directly with the food of the patient's diet. For oral therapeutic administration, the compounds may be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. For compositions suitable for administration to humans, the term “excipient” is meant to include, but is not limited to, those ingredients described in Remington: The Science and Practice of Pharmacy, Lippincott Williams & Wilkins, 21st ed. (2006) (hereinafter Remington's), which is herein incorporated by reference in its entirety.

The compounds may be combined with a fine inert powdered carrier and inhaled by the subject or insufflated. Such compositions and preparations should contain at least 0.1% compounds. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2% to about 60% of the weight of a given unit dosage form. The amount of compounds in such therapeutically useful compositions is such that an effective dosage level will be obtained.

The tablets, troches, pills, capsules, and the like may also contain the following: binders such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, fructose, lactose or aspartame or a flavoring agent such as peppermint, oil of wintergreen, or cherry flavoring may be added. When the unit dosage form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier, such as a vegetable oil or a polyethylene glycol. A syrup or elixir may contain the active compound, sucrose or fructose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring such as cherry or orange flavor.

Various other materials may be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or capsules may be coated with gelatin, wax, shellac or sugar and the like. Of course, any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed.

In addition, the compounds may be incorporated into sustained-release preparations and devices. For example, the compounds may be incorporated into time release capsules, time release tablets, and time release pills. In some embodiments, the composition is administered using a dosage form selected from the group consisting of effervescent tablets, orally disintegrating tablets, floating tablets designed to increase gastric retention times, buccal patches, and sublingual tablets.

The compounds may also be administered intravenously or intraperitoneally by infusion or injection. Solutions of the compounds can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations can contain a preservative to prevent the growth of microorganisms.

The pharmaceutical dosage forms suitable for injection or infusion can include sterile aqueous solutions or dispersions or sterile powders comprising the compounds which are adapted for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes. In all cases, the ultimate dosage form should be sterile, fluid and stable under the conditions of manufacture and storage. The liquid carrier or vehicle can be a solvent or liquid dispersion medium comprising, for example, water, ethanol, a polyol (for example, glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, nontoxic glyceryl esters, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions or by the use of surfactants.

The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, buffers or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions are prepared by incorporating the compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filter sterilization. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze drying techniques, which yield a powder of the active ingredient plus any additional desired ingredient present in the previously sterile-filtered solutions.

For topical administration, the compounds may be applied in pure form. However, it will generally be desirable to administer them to the skin as compositions or formulations, in combination with a dermatologically acceptable carrier, which may be a solid or a liquid.

Useful solid carriers include finely divided solids such as talc, clay, microcrystalline cellulose, silica, alumina and the like. Other solid carriers include nontoxic polymeric nanoparticles or microparticles. Useful liquid carriers include water, alcohols or glycols or water/alcohol/glycol blends, in which the compounds can be dissolved or dispersed at effective levels, optionally with the aid of non-toxic surfactants. Adjuvants such as fragrances and additional antimicrobial agents can be added to optimize the properties for a given use. The resultant liquid compositions can be applied from absorbent pads, used to impregnate bandages and other dressings, or sprayed onto the affected area using pump-type or aerosol sprayers.

Thickeners such as synthetic polymers, fatty acids, fatty acid salts and esters, fatty alcohols, modified celluloses or modified mineral materials can also be employed with liquid carriers to form spreadable pastes, gels, ointments, soaps, and the like, for application directly to the skin of the user.

Examples of useful dermatological compositions which can be used to deliver the compounds to the skin are known to the art; for example, see Jacquet et al. (U.S. Pat. No. 4,608,392), Geria (U.S. Pat. No. 4,992,478), Smith et al. (U.S. Pat. No. 4,559,157) and Wortzman (U.S. Pat. No. 4,820,508), all of which are hereby incorporated by reference.

Useful dosages of the compounds of formula I can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see U.S. Pat. No. 4,938,949, which is hereby incorporated by reference.

For example, the concentration of the compounds in a liquid composition, such as a lotion, can be from about 0.1-25% by weight, or from about 0.5-10% by weight. The concentration in a semi-solid or solid composition such as a gel or a powder can be about 0.1-5% by weight, or about 0.5-2.5% by weight.

The amount of the compounds required for use in treatment will vary not only with the particular salt selected but also with the route of administration, the nature of the condition being treated and the age and condition of the patient and will be ultimately at the discretion of the attendant physician or clinician.

Effective dosages and routes of administration of agents of the invention are conventional. The exact amount (effective dose) of the agent will vary from subject to subject, depending on, for example, the species, age, weight and general or clinical condition of the subject, the severity or mechanism of any disorder being treated, the particular agent or vehicle used, the method and scheduling of administration, and the like. A therapeutically effective dose can be determined empirically, by conventional procedures known to those of skill in the art. See, e.g., The Pharmacological Basis of Therapeutics, Goodman and Gilman, eds., Macmillan Publishing Co., New York. For example, an effective dose can be estimated initially either in cell culture assays or in suitable animal models. The animal model may also be used to determine the appropriate concentration ranges and routes of administration. Such information can then be used to determine useful doses and routes for administration in humans. A therapeutic dose can also be selected by analogy to dosages for comparable therapeutic agents.

In some embodiments, the pharmaceutical compositions described herein contain a therapeutically effective dose of the compound. The term “effective amount” or “therapeutically effective amount,” as used herein, refers to the amount of the active compound that is effective to achieve its intended purpose after a single dose, wherein a single dose comprises one or more dosage units, or after a course of doses, e.g., during or at the end of the treatment period. Thus, for example, the term “therapeutically effective amount” of the compounds disclosed herein, when used in a method of treating a cancer, refers to that dose of the compound that lessens or prevents the occurrence of cancer when administered to a mammal in need of such treatment. The therapeutically effective amount will vary depending on the needs of the subject, but this amount can readily be determined by one of skill in the art, for example, a physician.

The particular mode of administration and the dosage regimen will be selected by the attending clinician, taking into account the particulars of the case (e.g., the subject, the disease, the disease state involved, and whether the treatment is prophylactic). Treatment may involve daily or multi-daily doses of compound(s) over a period of a few days to months, or even years.

In general, however, a suitable dose will be in the range of from about 0.001 to about 100 mg/kg, e.g., from about 0.01 to about 100 mg/kg of body weight per day, such as above about 0.1 mg per kilogram, or in a range of from about 1 to about 10 mg per kilogram body weight of the recipient per day. For example, a suitable dose may be about 1 mg/kg, 10 mg/kg, or 50 mg/kg of body weight per day.

The compounds are conveniently administered in unit dosage form; for example, containing 0.05 to 10000 mg, 0.5 to 10000 mg, 5 to 1000 mg, or about 100 mg of active ingredient per unit dosage form. In some embodiments, the dosage unit contains about 1 mg, about 10 mg, about 25 mg, about 50 mg, about 75 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, about 300 mg, about 350 mg, about 400 mg, about 450 mg, about 500 mg, about 750 mg, or about 1000 mg of active ingredient.

The compounds can be administered to achieve peak plasma concentrations of, for example, from about 0.5 to about 75 μM, about 1 to 50 μM, about 2 to about 30 μM, or about 5 to about 25 μM. Exemplary desirable plasma concentrations include at least or no more than 0.25, 0.5, 1, 5, 10, 25, 50, 75, 100 or 200 μM. For example, plasma levels may be from about 1 to 100 micromolar or from about 10 to about 25 micromolar. This may be achieved, for example, by the intravenous injection of a 0.05 to 5% solution of the compounds, optionally in saline, or orally administered as a bolus containing about 1-100 mg of the compounds. Desirable blood levels may be maintained by continuous infusion to provide about 0.00005-5 mg per kg body weight per hour, for example at least or no more than 0.00005, 0.0005, 0.005, 0.05, 0.5, or 5 mg/kg/hr. Alternatively, such levels can be obtained by intermittent infusions containing about 0.0002-20 mg per kg body weight, for example, at least or no more than 0.0002, 0.002, 0.02, 0.2, 2, 20, or 50 mg of the compounds per kg of body weight.

The compounds may conveniently be presented in a single dose or as divided doses administered at appropriate intervals, for example, as two, three, four or more sub-doses per day. The sub-dose itself may be further divided, e.g., into a number of discrete loosely spaced administrations; such as multiple inhalations from an insufflator.

IV. Methods of Treating, Assays, and Kits

Some embodiments of the present invention are directed to methods of using the compounds described herein. These compounds, as illustrated in the examples below and throughout the specification, are useful in inhibiting the geranylgeranylation of signaling proteins by inhibiting the activity of at least GGTase I. However, because GGTIs such as those described herein can inhibit geranylgeranylation of a number of signaling proteins the compounds described herein are effective for the treatment of a wide range of human cancers. For example, mP5-H6 inhibits proliferation of a leukemic cell line (Jurkat), breast cancer cell lines (BT474 and MDA-MB231) and pancreatic cancer cell lines (Panc-I and MiaPaCa2).

Pancreatic cancer is of particular interest, as recent studies (Lim, K-H et al., Current Biology 16, 2385; Lim, K-H et al., Cancer Cell 7, 533) have established the importance of RalA and RalB proteins (both are geranylgeranylated) in pancreatic cancer. RalA is commonly activated in a panel of cell lines from pancreatic cancer. Studies using siRNA showed that inhibition of RalA reduced tumor growth. RalB is found to be important for metastasis. Interestingly, the RalA activation occurs downstream of K-ras activation that is seen in more than 80% of pancreatic cancer cases. Since K-ras prenylation can be inhibited by the combination of GGTI and FTI, GGTIs may be particularly important for pancreatic cancer.

Breast cancer is also of interest, as GGTIs have been shown to inhibit proliferation of breast cancer cells (Vogt, A. et al., J. Biol. Chem. 272, 27224). This is accompanied by the accumulation of G1 phase cells and the increase of p21. In addition, a geranylgeranylated protein Rac3 is reported to be overactivated in breast cancer cells (Mira J-P et al., PNAS 97, 185). Finally, inhibition of RhoA or RhoC by siRNA inhibited proliferation and invasiveness of breast cancer cells in vitro and in vivo (Pille, J-Y et al., Molecular Therapy 11, 267).

GGTIs may also be valuable in inhibiting cancer metastasis. This is based on the findings that geranylgeranylated proteins play important roles in metastasis. In addition to RalB discussed above, another geranylgeranylated protein RhoC plays essential roles in cancer metastasis (Hakem A. et al., Genes & Dev. 19, 1974; Clark, E. A. et al., Nature 406, 532).

Accordingly, the compounds can be used in methods of treating cancer. In some embodiments, the method of treating cancer involves inhibiting a protein prenyltransferase by administering the compound or salt described herein to a subject in need of treatment. The methods of treating cancer can be applied to any cancer that is activated through a signaling pathway incorporating GGTas I. For example, Rho protein activation, e.g., RhoA and Rac in cancer cells. In some embodiments, the cancer is selected from the group consisting of pancreatic, leukemia, breast, and prostate. In some embodiments, the cancer is selected from the group consisting of pancreatic, leukemia, breast, prostate, colon, ovarian, lung, and stomach cancer.

The compounds described herein are also useful in methods of inhibiting the activity of GGTase I by administering the compounds described herein to a cell. These methods can be applied either in vivo or in vitro. For example, these compounds can be used for therapeutic purposes associated with inhibiting the activity of GGTase I in a subject in need of treatment thereof. These compounds can also be used in research methods designed to develop such therapeutics. For example, as part of a library screening as described herein.

The compounds described herein are also useful in methods of cytostatically inhibiting the growth of a cancer cell. These methods can be used as a stand alone therapeutic or in conjunction with a cytotoxic treatment or a surgical procedure. The compounds described herein can be administered following surgery to remove a tumor or following chemotherapy designed to kill the tumor cells to control the growth of any cancer cells that these treatments may have missed. These compounds, when administered in these embodiments, may function as a preventative measure designed to reduce the likelihood of remission.

The compounds herein are also useful in assays for measuring the GGTase I inhibiting activity of a compound. For example, the compounds disclosed herein can be used as controls to evaluate new compounds for potential GGTase I inhibiting activity. The compounds disclosed herein can be used as part of assays to determine therapeutic compounds for use in the methods disclosed herein as well.

The invention also provides kits comprising a compound of the invention in the form of a pharmaceutically acceptable dosage form or as a compound. These kits can include one or more containers filled with one or more of the ingredients of the pharmaceutical dosage forms.

In some embodiments, the kit comprises a container for the dosage form or compound. Suitable containers include, for example, a bottle, a box, a blister card, a foil packet, or a combination thereof. Optionally, the kit also contains directions for properly administering the dosage form or for properly using the compound, for example, as part of an assay. The kits can also be designed in a manner such that they are tamper resistant or designed to indicate if tampering has occurred. Optionally, the kit can contain the dosage form or compound with another pharmaceutical composition or compound, for example, an FTI.

Optionally associated with the container(s) in the kits can be a notice or printed instructions. Such printed instructions can be in a form prescribed by a governmental agency regulating the manufacture, use, or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of the manufacture, use, or sale for human administration to treat a condition that could be treated by the compounds and dosage forms described herein. In some embodiments, the kit further comprises printed matter, which, e.g., provides information on the use of the dosage form to treat a condition or disease or a pre-recorded media device which, e.g., provides information on the use of the dosage form to treat a condition or disease, or a planner.

“Printed matter” can be, for example, one of a book, booklet, brochure or leaflet. The printed matter can describe the use of the dosage forms described herein to treat a condition or disease, for example, to treat a cancer involving GGTase I modification of proteins. Possible formats include, but are not limited to, a bullet point list, a list of frequently asked questions (FAQ) or a chart. Additionally, the information to be imparted can be illustrated in non-textual terms using pictures, graphics, or other symbols.

“Pre-recorded media device” can be, for example, a visual media device, such as a videotape cassette, a DVD (digital video disk), filmstrip, 35 mm movie, or any other visual media device. Alternately, pre-recorded media device can be an interactive software application, such as a CD-ROM (compact disk-read only memory) or floppy disk. Alternately, pre-recorded media device can be, for example, an audio media device, such as a record, audiocassette, or audio compact disk. The information contained on the pre-recorded media device can describe the use of the dosage forms and compounds described herein to treat a condition or disease, for example, to treat a cancer involving GGTase I modification of proteins.

A “planner” can be, for example, a weekly, a monthly, a multi-monthly, a yearly, or a multi-yearly planner. The planner can be used as a diary to monitor dosage amounts, to keep track of dosages administered, or to prepare for future events wherein taking a regularly administered dosage form as described herein. Alternately, the planner can be a calendar which will provide a means to monitor when a dosage has been taken and when it has not been taken. This type of planner will be particularly useful for patients having unusual schedules for administering medication to themselves. Additionally, the planner can be useful for the elderly, children, or other patient group who may administer medication to themselves and may become forgetful. One skilled in the art will appreciate the variety of planning tools that would be appropriate for use with compounds and dosage forms described herein.

The kit can also include a container for storing the other components of the kit. The container can be, for example, a bag, box, envelope or any other container that would be suitable for use with the compounds and dosage forms described herein. Preferably, the container is large enough to accommodate each component and/or any administrative devices that may be accompany the dosage form of the present invention. However, in some cases, it may be desirable to have a smaller container which can be hidden in a patient's pocketbook, briefcase, or pocket.

In some embodiments, the present invention includes a kit comprising a pharmaceutical dosage form described herein. In some embodiments, the kit further comprises printed instructions for its use. In some embodiments, the kit further comprises a printed matter, a pre-recorded media device, or a planner describing the use of the pharmaceutical dosage form of the present invention to treat or prevent a condition which could be aided by taking the compositions disclosed herein.

In some aspects, the present invention provides a method of delivering a pharmaceutical dosage form described herein, to a patient in need thereof, the method comprising:

(a) registering in a computer readable storage medium the identity of a physician permitted to prescribe the pharmaceutical dosage form; (b) providing the patient with counseling information concerning a risk attendant to the pharmaceutical dosage form; (c) obtaining informed consent of the patient to receive the pharmaceutical dosage form despite the risk; (d) registering the patient in the computer readable medium after obtaining the informed consent; and (e) permitting the patient access to the pharmaceutical dosage form.

In some embodiments of this method, the access to the pharmaceutical dosage form is a prescription.

Still other aspects of the present invention include a method of educating a consumer regarding the pharmaceutical dosage forms described herein, the method comprising distributing the oral pharmaceutical dosage form to a consumer with consumer information at a point of sale.

In some embodiments, the consumer information is presented in a format selected from the group consisting of: English language text, a foreign language text, a visual image, a chart, a telephone recording, a website, and access to a live customer service representative. In some embodiments, the consumer information is a direction for use, appropriate age use, indication, contraindication, appropriate dosing, warning, telephone number, or website address.

In some embodiments, the method of educating the consumer further comprises providing professional information to a relevant person in a position to answer a consumer question regarding the pharmaceutical dosage form. In some embodiments, the relevant person is a physician, physician assistant, nurse practitioner, pharmacist, or customer service representative.

In some embodiments, the distributing of the pharmaceutical dosage form is to a location with a pharmacist or a health care provider.

Example 1

We report the first example of phosphine catalysis of polymer-bound allenoates and a combinatorial library approach to the development of potent inhibitors of protein geranylgeranyltransferase type I (GGTase-I).

A collection of 138 heterocycles was screened for their ability to inhibit the activity of human GGTase-I to geranylgeranylate K-Ras4B or RhoA. Purified GGTase-1 was incubated with its substrate protein K-Ras4B or RhoA, [³H]GGPP, and the 138 compounds. After 30 min, the degree of incorporation of tritiated geranylgeranyl groups was measured using a scintillation counter.

A number of compounds were identified as GGTIs including the following compounds numbered 1 and 2:

This discovery of promising lead GGTI compounds and their moderate activity warranted the development of efficient and rapid syntheses and evaluations of analogous structures in the search for better inhibitors; we envisioned a short, modular synthetic route (Scheme 1), using SynPhase™ lanterns as the solid support. Validation of the synthetic route on the polymer support commenced with formation of resin-bound allenoates 5. The loading of allenoic acids onto solid supports has not been reported previously. The allenoic acids 4 were coupled to the benzyl alcohol units of the SynPhase-PS lanterns grafted with Wang resin 3 using Mukaiyama's reagent and Hünig's base for 4a/b or Et₃N for 4c/d. The direct use of an unmodified Wang resin minimizes the number of synthetic operations run on solid support. In addition, our strategy enabled simple trifluoroacetic acid (TFA)-mediated cleavage to release the carboxylic acid group, a key functional group in our GGTIs.

The phosphine-catalyzed annulation between solid-bound polymer-supported allenoates 5 and N-tosylimines proceeded smoothly. The allenoates 5a and 5b were treated with N-tosyltolualdimine and 50 mol % of PPh₃ (for 5a) or PBu₃ (for 5b) in benzene at 60° C. to provide the polymer-bound dihydropyrroles 6. Tetrahydropyridines 7 were formed from the reactions of 5c and 5d with N-tosyltolualdimine in the presence of 50 mol % of PBu₃ at room temperature for 2 and 4 days, respectively. Heterocycles 6 and 7 were cleaved from the resin using 2.5% TFA in DCM to provide the carboxylic acids 8 and 9 in 91-94% yield (based on a theoretical loading of 15 mmol/lantern) with high diastereoselectivities (dr=99:1 for 8b; 93:7 for 9b) after chromatographic purification.

The α,β-unsaturated enoate functionalities in 6 and 7 were utilized to further increase the modularity and number of analogs. For example, the Michael additions of thiols to 6 and 7 using n-butyllithium as base provided 10 and 11, respectively, which upon TFA-mediated cleavage yielded 12 and 13, respectively, in 77-95% yield (Scheme 2). These two-step sequences occurred with high diastereoselectivities, providing the pentasubstituted pyrrolidine 12 and the tetrasubstituted piperidine 13 as single diastereoisomeric products. Apparently, thiols added opposite to the preexisting substituents in both the dihydropyrrole 6 and the tetrahydropyridine 7. Interestingly, however, the protonation of the resulting α-carbanions occurred anti (for 10) and syn (for 11) to the added β-mercapto groups.

Having successfully established the solid phase reaction conditions, we next prepared the α- and γ-substituted allenoic acids building blocks (Scheme 3). The reactions between the phosphorane 14 and the acid chlorides 15 (1 equiv) in the presence of Et₃N (1 equiv) provided the allenoates 16, which were hydrolyzed into γ-substituted allenoic acids A. Phosphorane 14 was treated with the alkyl halides 17 to give the phosphonium salts 18, which we converted to the α-substituted allenoates 19 upon treatment with Et₃N (2 equiv) and acetyl chloride (1 equiv). α-Substituted allenoic acids B were prepared through saponification of the esters 19. The N-sulfonylimines C were formed simply through azeotropic removal of water from a mixture of the appropriate sulfonamide 20, aldehyde 21, and BF₃.Et₂ under reflux in toluene. Chart 1 presents the building blocks synthesized as illustrated in Scheme 3 and the commercially available thiol building blocks D.

The building blocks were tested so that only the ones that provided high purity and stereoselectivity (as judged from ¹H NMR spectra and LCMS analyses) for their crude cleavage products would be used in the synthesis of the GGTI analog library. Eleven γ-substituted allenoic acids A and 12 α-substituted allenoic acids B were loaded and reacted with imine C02 in the presence of a catalytic amount of phosphine, as indicated in Scheme 1. After cleavage with TFA and analysis (¹H NMR and LCMS spectra) of the purity and diastereoselectivity of the 23 annulation products 6 and 7, we found that each of the allenoic acids, except for A10, yielded a single identifiable compound (dr≧12:1; ¹H NMR) in high purity (72-100%; LCMS/UV210). The resin-bound allenoates derived from allenoic acids A01, A05, B01, and B05 were selected to assess the reactivity and stereoselectivity of 46 imines in phosphine-catalyzed annulations (because A01, A02-A11, B01, and B02B12 required different annulation reaction conditions). Using the criteria of >70% purity and >9:1 dr, we selected 30 (of 46) imine building blocks for allenoate A01, 21 for A05, 25 for B01, and 31 for B05.

Chart 1. Eleven γ-substituted allenoic acids A, 12α-substituted allenoic acids B, 46 N-sulfonimines C, and 32 thiols D.

For Michael addition of the thiols, all three building blocks were tested as follows: To select suitable allenoic acids, the 23 annulation products synthesized above were subjected to Michael addition using benzenethiol, toluenethiol, or benzyl thiol. Analysis of the cleaved products indicated that eight (of 23) allenoic acids were suitable candidates. For imine selection, the annulation products of 46 imines with A05 and B01 were tested because the allenoic acids A01-04 and B02-B12 were excluded from the Michael addition sequence. The number of imines selected was 25 (of 46) for A05 and 21 for B01. The annulation products 6 and 7 (Scheme 2) were used to select the thiols; the various thiols required different reaction times and temperatures. Upon extensive optimization, 19 (of 32) thiols for dihydropyrrole 6 and 17 for tetrahydropyridine 7 were selected. The combination of these selected building blocks resulted in the preparation of 4288 compounds.

Using the chosen building blocks, we commenced the split-pool syntheses of the 4288 GGTI analogs on the SynPhase lanterns. Tagging was performed by inserting colored spindles and cogs into the lanterns prior to synthesis of the library.¹⁴ Twenty-three allenoic acids A and B were loaded onto the Wang resin 3 using Mukaiyama's reagent (Scheme 1). The resulting allenoate-loaded lanterns 5 were pooled and split into a number of flasks corresponding to the number of imines for each group of allenoic acids (A01, A02-A11, B01, and B02-B12). Sets of 240 dihydropyrrole-loaded lanterns 6 and 366 tetrahydropyridine-loaded lanterns 7 were placed aside for cleavage. Sets of 3325 dihydropyrrole-bound lanterns 6 and 357 tetrahydropyridine-bound lanterns 7 were further divided into 19 and 17 flasks, respectively, and subjected to the thiol Michael reactions (Scheme 2).

The 4288 lanterns were inserted into 4288 vials and treated with 2.5% TFA in CH₂Cl₂ for 12 h; the lanterns were then removed and rinsed with CH₂Cl₂. The resulting solution was concentrated and further co-evaporated with CHCl₃ to effectively remove TFA. The cleaved compounds were weighed and redissolved in CHCl₃; a portion (2 μmol) of each compound was transferred into 54 96-well plates (80 compounds per well; two columns of wells in each plate were left empty to accommodate controls in subsequent assays) and the solvents were left to evaporate. The products were redissolved in DMSO and analyzed in the same assay for activity against GGTase-I.

In the in vitro assay, active compounds were sought for their ability to inhibit the geranylgeranylation of both RhoA and K-Ras4B. The two compounds (22 and 23) that exhibited some of the highest activities obtained so far are shown in (a) below. These compounds exhibit specific inhibition of GGTase-I; i.e., they did not inhibit FTase at concentrations at which they inhibited GGTase-I by more than 90%.

FIG. 33 shows Western blot of the cell lysate qualitatively detecting the amount of gernanylgeranylated Rheb. The descriptors P and U designate processed and unprocessed Rheb, respectively.

Finally, we investigated in vivo effects of compounds 22 (also known as UC-22) and 23 (also known as UC-23). Human embryonic kidney (HEK) 293 cells were transfected with the Rheb-CSVL construct that expresses the geranylgeranylated form of the Rheb protein. Inhibition of the geranylgeranylation of this protein can be detected from a shift in its mobility on SDS polyacrylamide gel; the unprocessed form appears as a slowly migrating band. FIG. 33 indicates that treatment of the cells with compound 22 or 23 resulted in the appearance of a slowly migrating band (cf. the DMSO lane with lanes compounds 22 and 23); known GGTIs (GGTI298, GGTI2166) were used as controls. These results suggest that compounds 22 and 23 inhibit geranylgeranylation within the cell.

Example 2

As illustrated in FIGS. 20A-20C, compounds P3-E5 and P5-H6 specifically inhibit GGTase I. The graph illustrates the effect of P3-E5 and P5-1-16 on the enzymatic activity of GGTase-I (A), FTase (B) GGTase-II (C). Varying concentrations of the two compounds were added to each enzyme reaction. The FTase (protein farnesyltransferase) assay was carried out using K-Ras4B as a substrate protein, FTase (JENA Bioscience, San Diego, Calif.) and [3]farnesyl pyrophosphate. Incubation was for 30 min at 37 C.

The GGTase-I assay was carried out using RhoA as a substrate protein, GGTase-I (JENA Bioscience) and [3H]geranylgeranyl pyrophosphate. Incubation was for 30 min at 37 C. GGTase-H (or RabGGTase) assay was carried out using YPT1 as a substrate protein, GGTase-H (Calbiochem, San Diego, Calif.) plus REP1 (Calbiochem) and [3H]geranylgeranyl pyrophosphate. Incubation was for 30 min at 37 C. FIGS. 20D-20F show the three dimensional structure of GGTase I (D), FTsse (E) and GGTase II (F) which can be obtained from X-ray diffraction studies of protein crystals.

Example 3

As illustrated in FIGS. 21A-21D, P3-E5 and P5-H6 compete with a substrate protein but do not compete with GGPP. The graphs in FIG. 21 show double reciprocal plots obtained from substrate velocity curves for the inhibition of GGTase-I by P3-E5 (left) and P5-H6 (right). The upper figures show varying GGPP concentrations with a fixed RhoA protein concentration were used. The lower figures show varying RhoA protein concentrations with a fixed GGPP concentration was used. The following scale was used to prepare the graphs: Y-axis: 1/v, fmol/min. X-axis: 1/s, mM.

Example 4

As illustrated in FIGS. 22A and 22B, P3-E5 inhibits geranylgeranylation in cells. Human embryonic kidney (HEK) 293 cells expressing Myc-HA tagged-Rheb-CVSL (upper) or Myc-HA tagged-Rheb-WT (lower) were treated with P3-E5 for 48 hours and then lysed. The cell lysates were run on a SDS polyacrylamide gel and immunoblotted using anti-Myc or anti-Actin antibody. The descriptors P and U indicate processed and unprocessed Rheb, respectively. Similar results hay been obtained with P5-H6 but are not depicted in FIG. 22.

Example 5

As illustrated in FIG. 23, P3-E5 and P5-H6 inhibit proliferation of K562 cells. K562 cells are a cell line of human erythroleukemia cells. The K562 cells were treated with P3-E5, P5-H6 or GGTI-298 (a known GGTI compound illustrated in FIG. 27) for 72 hours and then cell number was counted using cell counting kit-8 (Dojindo, Gaithersburg, Md.). Cell viability relative to the DMSO control and the known GGTI compound is plotted in FIG. 23. It can be seen that both P3-E5 and P5-H6 inhibit the growth of the K562 cells.

Example 6

As illustrated in FIG. 24A, P3-E5 induces G1 arrest in K562 cells. K562 cells were treated with indicated concentrations (mM) of P3-E5 (ranging from 0 to 10 mM) or GGTI-298 (ranging from 0 to 10 mM) for 48 hours. Cell cycle profiles were monitored by flow cytometry. Percentages of cells in each phase of the cell cycle are indicated by different colors. Red: G0/G1 phase. Black: S phase. Gray: G2/M phase. Similar results were obtained with P5-H6.

While not wishing to be bound to a single theory, FIG. 24B illustrates an exemplary mechanism to explain the cell cycle effect of GGTIs. RhoA is known to inhibit expression of p21WAF. GGTI may function by inhibiting geranylgeranylation of RhoA leading to the increase in p21WAF expression. This could result in G1 arrest.

Example 7

As illustrated in FIG. 25, mP5-H6 inhibits geranylgeranylation in vivo. Human embryonic kidney (HEK) 293 cells expressing Myc-HA tagged-Rheb-CVSL (upper) or Myc-HA tagged-Rheb-WT (lower) were treated with mP5-H6a (also referred to as mP5-H6), or GGTI-298 for 48 hours and then lysed. Lysates were run on a SDS polyacrylamide gel and immunoblotted with anti-Myc or anti-Actin antibody. Processed and unprocessed Rheb may be used in the method described in this example as shown in FIG. 22.

Example 8

As shown in FIG. 26, mP5-H6 exhibits increased potency to inhibit proliferation relative to P5416. Panc-1 cells (Pancreatic cancer cell line) and Jurkat cells (T-cell leukemia) were treated with 12.5 μM of P5-H6 or 12.5 μM of mP5-H6a for 72 hours. The cell number was counted as described in Example 5. The graph shows that mP5-H6a inhibits the growth of Panc-1 cells and Jurkat cells better than P5-H6.

The embodiments illustrated and discussed in this specification are intended only to teach those skilled in the art the best way known to the inventors to make and use the invention. Nothing in this specification should be considered as limiting the scope of the present invention. All examples presented are representative and non-limiting. The embodiments of the invention may be modified or varied, without departing from the invention, as appreciated by those skilled in the art in light of the above teachings. It is therefore to be understood that, within the scope of the claims and their equivalents, the invention may be practiced otherwise than as specifically described. 

1. A compound having the formula

wherein J is hydrogen or is 1-2 substituents selected from the group consisting C₁-C₃ alkyl and halogen, wherein G is

wherein E is selected from the group consisting of hydrogen, C₁-C₃ alkyl, and halogen, wherein W is selected from the group consisting of cyclic, linear, or branched alkyl of from 2 to 8 carbons, unsubstituted phenyl, and phenyl substituted with C₁-C₃ alkyl, hydrogen, or halogen, wherein X—Y is selected from the group consisting of

wherein A is selected from the group consisting of

and —CO₂M; wherein M is selected from the group consisting of hydrogen and alkyl of from 1 to 2 carbons, “wherein n is between 0 and 3 carbons; wherein R is any alpha-substituent of an amino acid; wherein Z is S—U; and wherein U is selected from the group consisting of alkyl of from 2 to 10 carbons; and salts of the compound.
 2. A compound or salt thereof having the formula of claim 1, wherein X—Y is

and A is CO₂H.
 3. The compound or salt thereof of claim 2, wherein W is tert-butyl and E is methyl.
 4. The compound or salt thereof of claim 2, wherein J is one halogen substituent.
 5. The compound or salt thereof of claim 2, wherein W is tert-butyl, E is methyl, and J is chlorine.
 6. A compound or salt thereof having the formula of claim 1, wherein X—Y is

and A is CO₂H.
 7. The compound or salt thereof of claim 6, wherein W is phenyl substituted with halogen and E is methyl.
 8. The compound or salt thereof of claim 6, wherein and J is one halogen substituent.
 9. The compound or salt thereof of claim 6, wherein W is phenyl substituted with chlorine, E is methyl, and J is chlorine.
 10. A compound or salt thereof having the formula of claim 1, wherein X—Y is

and A is


11. The compound of claim 10, wherein W is tert-butyl and E is methyl.
 12. The compound of claim 10, wherein J is one halogen substituent.
 13. The compound of claim 10, wherein W is tert-butyl, E is methyl, and J is chlorine.
 14. The compound or salt thereof of claim 1, wherein G is


15. A compound or salt thereof having the formula:


16. A compound or salt thereof having the formula:


17. A compound having the formula:


18. A compound of claim 1, wherein the compound or a salt thereof inhibits the activity of a protein prenyltransferase.
 19. A pharmaceutical composition comprising the compound or salt of claim 1 and a pharmaceutically acceptable carrier or diluent.
 20. A method comprising administering the compound or salt of claim 1 to a cell in an amount sufficient to inhibit the activity of GGTase I.
 21. A method comprising administering a compound or salt of claim 1 in an amount sufficient to inhibit the growth of a cancer cell.
 22. The method of claim 21, wherein the cancer is selected from the group consisting of pancreatic, leukemia, breast, lung, colon, ovarian, stomach, and prostate cancer.
 23. The method of claim 21, wherein the cancer cell comprises GGTase I modified proteins.
 24. A method comprising administering to a subject in need of treatment for a cancer the pharmaceutical composition of claim 10 in an amount sufficient to inhibit the activity of a protein prenyltransferase.
 25. The method of claim 24, wherein the cancer is selected from the group consisting of pancreatic, leukemia, breast, lung, colon, ovarian, stomach, and prostate cancer.
 26. The method of claim 24, wherein the protein prenyltransferase is GGTase I.
 27. The method of claim 24, wherein the cancer cell comprises GGTase I modified proteins.
 28. A method comprising measuring the GGTase I inhibiting activity of a compound of claim
 1. 